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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412341생성일: 2026년 10월 25일

Triethylamine → 1-(3-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)-3-n-hexylurea

https://huagongshe.com/reaction/412341

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Hexyl isocyanateHCID 75659—
반응물5-[4-[6-(3-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochlorideHCID 86587772—
용매DimethylformamideHCID 6228—
생성물1-(3-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl)-3-n-hexylureaHCID 1853757667.8%

반응 단계

A mixture of 5-[4-[6-(3-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (400 mg), n-hexyl isocyanate (280 mg), triethylamine (153 mg) and anhydrous N,N-dimethylformamide (8 ml) was stirred at room temperature for 7 hours and then allowed to stand overnight. The reaction mixture was concentrated and partitioned between ethyl acetate and water. The extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and then concentrated. The residue was chromatographed on a silica gel column using ethyl acetate/n-hexane=3:1→4:1→ethyl acetate→ethyl acetate:methanol=15:1 as the eluant. The product was recrystallized from ethyl acetate to afford the title compound (298 mg, mp 143.7-146.9° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562849B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-d9d18430d92b42858282cf5180041a96
출처 메모uspto-grants-2003_05